Catalog Number

ROSAS00159

Brand Name

GUIDE WIRE NAV REF

Version/Model Number

174028-00

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K182848,K192173

Product Code

OLO

Product Code Name

Orthopedic Stereotaxic Instrument

Public Device Record Key

d46ba2e0-5107-4b51-99ae-9f3df82af46c

Public Version Date

July 12, 2022

Public Version Number

3

DI Record Publish Date

June 08, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-